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Volumn 47, Issue 22, 2006, Pages 3733-3736

Enantioselective hydrogenation of diaryl-substituted α,β-unsaturated nitriles

Author keywords

[No Author keywords available]

Indexed keywords

ARPROMIDINE; HISTAMINE H2 RECEPTOR AGONIST; NITRILE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; RUTHENIUM COMPLEX;

EID: 33646115804     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.03.115     Document Type: Article
Times cited : (16)

References (33)
  • 18
    • 33845281011 scopus 로고
    • For detailed mechanistic studies of this reaction, see:
    • For detailed mechanistic studies of this reaction, see:. Landis C.R., and Halpern J. J. Am. Chem. Soc. 109 (1987) 1746
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 1746
    • Landis, C.R.1    Halpern, J.2
  • 27
    • 33646116499 scopus 로고    scopus 로고
    • Jones, Z. A.; Ph.D. Dissertation, University of Cambridge, 2005.
  • 28
    • 33646078273 scopus 로고    scopus 로고
    • note
    • The formation of stable seven-membered chelate rings of the ruthenium catalyst and the Z-isomer cannot be ruled out as it was observed that ruthenium(II) in these solutions was considerably less sensitive to oxygen than the corresponding systems containing the E-isomer.
  • 30
    • 33646113795 scopus 로고    scopus 로고
    • note
    • Using pyridine as a stoichiometric or catalytic additive did not increase conversion with unreactive substrates. Therefore, pyridine substituents most likely serve as coordination sites.
  • 31
    • 33646119813 scopus 로고    scopus 로고
    • note
    • 3).
  • 32
    • 0347745231 scopus 로고    scopus 로고
    • 4 to the corresponding amine (80%, no racemization observed), being previously described in enantiomerically pure form:
    • 4 to the corresponding amine (80%, no racemization observed), being previously described in enantiomerically pure form:. Zabel M., Breu J., Rau F., Range K.-J., Krey A., Uffrecht A., and Buschauer A. Acta Cryst. C56 (2000) 250
    • (2000) Acta Cryst. , vol.C56 , pp. 250
    • Zabel, M.1    Breu, J.2    Rau, F.3    Range, K.-J.4    Krey, A.5    Uffrecht, A.6    Buschauer, A.7
  • 33
    • 0034988181 scopus 로고    scopus 로고
    • The configuration of all other products was assigned in analogy to these results
    • Schuster A., Götte C., Bernhardt G., and Buschauer A. Chirality 13 (2001) 285 The configuration of all other products was assigned in analogy to these results
    • (2001) Chirality , vol.13 , pp. 285
    • Schuster, A.1    Götte, C.2    Bernhardt, G.3    Buschauer, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.